3ygs

APAF-1 CARD IN COMPLEX WITH PRODOMAIN OF PROCASPASE-9

Method: X-RAY DIFFRACTION Dmax: 61.6 Å Quality: GOOD

1. Protein Identity and Related Structures Protein Identity & Related Structures

APOPTOTIC PROTEASE ACTIVATING FACTOR 1

Homo sapiens

UniProt O14727

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 1–95 Fragment:CASPASE RECRUITMENT DOMAIN (CARD) PROCASPASE 9 × 1 (P55211) X-RAY DIFFRACTION X-ray crystallization conditions:pH 7.5;pH 7.5 Resolution 2.50 Å R-free 0.299

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

13 other PDB entries and 19 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name APAF_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain C; PDBConstruct 1–95; UniProt 1–95

PROCASPASE 9

Homo sapiens

UniProt P55211

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain P; UniProt 1–96 Fragment:PRODOMAIN APOPTOTIC PROTEASE ACTIVATING FACTOR 1 × 1 (O14727) X-RAY DIFFRACTION X-ray crystallization conditions:pH 7.5;pH 7.5 Resolution 2.50 Å R-free 0.299

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

7 other PDB entries and 16 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CASP9_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain P; PDBConstruct 2–97; UniProt 1–96

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 3ygs

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3ygs
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3ygs
Deposition date deposition_date1999-05-08
Structure title titleAPAF-1 CARD IN COMPLEX WITH PRODOMAIN OF PROCASPASE-9
Keywords keywordsAPOPTOSIS, CASPASE ACTIVATION, CASPASE RECRUITMENT, RECOGNITION COMPLEX; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier18.64
Radius of gyration Rg (electron density) rg_electron17.77
Forward intensity I(0) i09543450.00
Molecular weight molecular_weight22202.0 kDa
Excluded volume excluded_volume27515 ų
Envelope volume envelope_volume31433 ų
Hydration-shell volume shell_volume15357 ų
Envelope diameter envelope_diameter59.8
Shell Rg shell_rg23.00
Envelope Rg envelope_rg17.98
Shape Rg shape_rg17.77
Total Rg total_rg18.55
Total atoms total_atoms1553
Residues n_residues192
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax61.6
Rg (real space) rg_real18.64
Rg uncertainty (real space) rg_real_error0.36
I(0) (real space) i0_real9.5430e+06
I(0) uncertainty (real space) i0_real_error1.1640e+05
Rg (reciprocal space) rg_reciprocal18.64
I(0) (reciprocal space) i0_reciprocal9543000.0000
Solution quality estimate total_estimate0.8749
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary21.1
Skewness Skewness skewness0.364
Kurtosis Kurtosis kurtosis-0.356
Angular range angular_range— – 0.4250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2326000.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.795; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.993; Smooth: 0.992

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 5 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd3ygsc_
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD
Domain ID domain_idd3ygsp1
Class classa — All alpha proteins
Fold Fold folda.77 — DEATH domain
Superfamily Superfamily superfamilya.77.1 — DEATH domain
Family Family familya.77.1.3 — Caspase recruitment domain, CARD
Domain ID domain_idd3ygsp2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (2 domains)

Domain ID domain_id3ygsC00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas
Domain ID domain_id3ygsP00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology533 — Death Domain, Fas
Homologous superfamily homologous superfamily10 — Death Domain, Fas

8. Citations (1)

9. Files and Curves (10)